Senior Clinical Field Specialist

JR United Kingdom; Lincoln; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading company in medical technology is seeking a Senior Clinical Research Specialist in Lincoln. The successful candidate will manage clinical trials for an innovative device that enhances heart attack treatment, training staff, ensuring compliance, and overseeing site management. The role demands expertise in clinical research and a strong background in GCP and ISO standards.

Qualifications

• Experience as Clinical Research Associate or Specialist in medical devices or CROs.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulatory standards.
• Experience in proctoring and site management preferred.

Responsibilities

• Train study staff on the correct use of the study device.
• Manage clinical trial activities from initiation to close-out.
• Conduct site visits to ensure compliance and data quality.

Skills

Organizational skills

Communication skills

Ability to work independently

Teamwork

Education

Bachelor’s degree in a relevant health science field

Master’s degree preferred

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, Lincoln

Client:

The Mullings Group

Location:

Lincoln, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

Job Views:

6

Posted:

26.06.2025

Expiry Date:

10.08.2025

Job Description:

In recent decades, treatment of heart attacks by minimally invasive percutaneous coronary intervention (PCI) has significantly improved patient outcomes. However, successful re-opening of narrow or blocked coronary arteries does not always restore blood flow to the entire heart muscle.

Our client is developing a first-in-class medical device that will diagnose MVO in real-time during PCI and serve as a treatment platform in the cath lab.

As they roll out their clinical trial across Europe, we are hiring a Senior Clinical Research Specialist to oversee and manage clinical trials, support proctoring activities, and take on advanced responsibilities related to the client's innovative technology.

Responsibilities:

• Train study staff on the correct use of the study device.
• Supervise site setup to ensure quality data collection.
• Maintain detailed records of proctoring activities.
• Support site staff during live clinical cases.
• Authorize sites for independent device use in collaboration with CPM.
• Participate in clinical cases to support device use.
• Manage clinical trial activities from initiation to close-out.
• Train staff on study procedures, software, and regulatory requirements.
• Conduct site visits to ensure compliance and data quality.
• Collaborate with investigators and CROs to resolve issues.

Regulatory Requirements Support:

• Assist with IRB submissions and audits.
• Ensure compliance with regulatory standards during inspections.

Data Management:

• Ensure accurate data collection and resolve discrepancies.

Qualifications:

• Bachelor’s degree in a relevant health science field; master’s preferred.
• Experience as Clinical Research Associate, Specialist, or similar role in medical devices or CROs.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulatory standards.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Ability to work independently and in teams.
• Proficiency in CTMS and EDC software.